Have questions? Visit https://www.reddit.com/r/SNPedia

rs374574638

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374574638(A;A)
Make rs374574638(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position3844977
GeneCEP104
is asnp
is mentioned by
dbSNPrs374574638
ebirs374574638
HLIrs374574638
Exacrs374574638
Varsomers374574638
Maprs374574638
PheGenIrs374574638
hapmaprs374574638
1000 genomesrs374574638
hgdprs374574638
ensemblrs374574638
gopubmedrs374574638
geneviewrs374574638
scholarrs374574638
googlers374574638
pharmgkbrs374574638
gwascentralrs374574638
openSNPrs374574638
23andMers374574638
23andMe allrs374574638
SNP Nexus

SNPshotrs374574638
SNPdbers374574638
MSV3drs374574638
GWAS Ctlgrs374574638
Max Magnitude0
ClinVar
Risk rs374574638(A;A)
Alt rs374574638(A;A)
Reference rs374574638(G;G)
Significance Pathogenic
Disease Joubert syndrome 25
Variation info
Gene CEP104
CLNDBN Joubert syndrome 25
Reversed 0
HGVS NC_000001.10:g.3761541G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000207197.1,